"ADAMTS9 Protein" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An ADAMTS protease that contains 15 THROMBOSPONDIN (TS) motifs. It cleaves the PROTEOGLYCANS AGGRECAN and VERSICAN and also functions in protein transport from the ENDOPLASMIC RETICULUM to the GOLGI APPARATUS.
| Descriptor ID |
D000071119
|
| MeSH Number(s) |
D08.811.277.656.675.374.102.500.968 D09.400.430.500.500.968 D12.776.395.033.500.968 D12.776.860.300.085.968
|
| Concept/Terms |
ADAMTS9 Protein- ADAMTS9 Protein
- A Disintegrin And Metalloproteinase With Thrombospondin Motifs 9 Protein
- ADAMTS-9 Protein
- ADAMTS 9 Protein
|
Below are MeSH descriptors whose meaning is more general than "ADAMTS9 Protein".
Below are MeSH descriptors whose meaning is more specific than "ADAMTS9 Protein".
This graph shows the total number of publications written about "ADAMTS9 Protein" by people in this website by year, and whether "ADAMTS9 Protein" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 0 | 1 | 1 |
| 2016 | 1 | 0 | 1 |
| 2019 | 3 | 0 | 3 |
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Below are the most recent publications written about "ADAMTS9 Protein" by people in Profiles.
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Wang LW, Nandadasa S, Annis DS, Dubail J, Mosher DF, Willard BB, Apte SS. A disintegrin-like and metalloproteinase domain with thrombospondin type 1 motif 9 (ADAMTS9) regulates fibronectin fibrillogenesis and turnover. J Biol Chem. 2019 06 21; 294(25):9924-9936.
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Nandadasa S, Kraft CM, Wang LW, O'Donnell A, Patel R, Gee HY, Grobe K, Cox TC, Hildebrandt F, Apte SS. Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis. Nat Commun. 2019 02 27; 10(1):953.
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Choi YJ, Halbritter J, Braun DA, Schueler M, Schapiro D, Rim JH, Nandadasa S, Choi WI, Widmeier E, Shril S, K?rber F, Sethi SK, Lifton RP, Beck BB, Apte SS, Gee HY, Hildebrandt F. Mutations of ADAMTS9 Cause Nephronophthisis-Related Ciliopathy. Am J Hum Genet. 2019 01 03; 104(1):45-54.
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Benz BA, Nandadasa S, Takeuchi M, Grady RC, Takeuchi H, LoPilato RK, Kakuda S, Somerville RPT, Apte SS, Haltiwanger RS, Holdener BC. Genetic and biochemical evidence that gastrulation defects in Pofut2 mutants result from defects in ADAMTS9 secretion. Dev Biol. 2016 08 01; 416(1):111-122.
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Nandadasa S, Nelson CM, Apte SS. ADAMTS9-Mediated Extracellular Matrix Dynamics Regulates Umbilical Cord Vascular Smooth Muscle Differentiation and Rotation. Cell Rep. 2015 Jun 16; 11(10):1519-28.